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dc.contributor.authorGuerrero, Rosa-
dc.contributor.authorVernia, Santiago-
dc.contributor.authorSanz, Raúl-
dc.contributor.authorAbreu-Rodríguez, Irene-
dc.contributor.authorAlmaraz, Carmen-
dc.contributor.authorGarcía-Hoyos, María-
dc.contributor.authorMichelucci, Roberto-
dc.contributor.authorTassinari, Carlo Alberto-
dc.contributor.authorRiguzzi, Patrizia-
dc.contributor.authorNobile, Carlo-
dc.contributor.authorSanz, Pascual-
dc.contributor.authorSerratosa, José M.-
dc.contributor.authorGómez-Garre, Pilar-
dc.identifier.citationPLoS ONE 6(6): e21294 (2011)es_ES
dc.description9 pages, 6 figures, PMID:21738631[PubMed]es_ES
dc.description.abstractLafora disease is an autosomal recessive form of progressive myoclonus epilepsy with no effective therapy. Although the outcome is always unfavorable, onset of symptoms and progression of the disease may vary. We aimed to identify modifier genes that may contribute to the clinical course of Lafora disease patients with EPM2A or EPM2B mutations. We established a list of 43 genes coding for proteins related to laforin/malin function and/or glycogen metabolism and tested common polymorphisms for possible associations with phenotypic differences using a collection of Lafora disease families. Genotype and haplotype analysis showed that PPP1R3C may be associated with a slow progression of the disease. The PPP1R3C gene encodes protein targeting to glycogen (PTG). Glycogen targeting subunits play a major role in recruiting type 1 protein phosphatase (PP1) to glycogen-enriched cell compartments and in increasing the specific activity of PP1 toward specific glycogenic substrates (glycogen synthase and glycogen phosphorylase). Here, we report a new mutation (c.746A>G, N249S) in the PPP1R3C gene that results in a decreased capacity to induce glycogen synthesis and a reduced interaction with glycogen phosphorylase and laforin, supporting a key role of this mutation in the glycogenic activity of PTG. This variant was found in one of two affected siblings of a Lafora disease family characterized by a remarkable mild course. Our findings suggest that variations in PTG may condition the course of Lafora disease and establish PTG as a potential target for pharmacogenetic and therapeutic approacheses_ES
dc.description.sponsorshipThis work was supported by grants from the Fundación Mutua Madrileña to PGG and RG, the Spanish Ministry of Education and Science (SAF2008-01907, SAF2007-61003) to PS and JMS and from the Generalitat Valenciana (Prometeo 2009/051) to PS.es_ES
dc.publisherPublic Library of Sciencees_ES
dc.relation.isversionofPublisher’s version-
dc.titleA PTG Variant Contributes to a Milder Phenotype in Lafora Diseasees_ES
dc.description.peerreviewedPeer reviewedes_ES
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